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J Fontcuberta

Showing results (141-150 of 172) with videos related to

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Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 24, 2009
SNP sets selection under mutual information criterion, application to F7/FVII datasetH Brunel, A Perera, A Buil, et al.
Stroke|August 30, 2003
Risk of ischemic stroke associated with functional thrombin-activatable fibrinolysis inhibitor plasma levelsA Santamaría, A Oliver, M Borrell, et al.
The Journal of Thoracic and Cardiovascular Surgery|October 1, 1995
Aprotinin versus desmopressin for patients undergoing operations with cardiopulmonary bypass. A double-blind placebo-controlled studyJ I Casas, I Zuazu-Jausoro, J Mateo, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|May 6, 2005
[Renal venous thrombosis in a neonate carrying the G20210A mutation of the prothrombin gene]G M Fraga Rodríguez, R Parody Porras, G Ginovart Galiana, et al.
Clinical Genetics|May 3, 2006
Genetic architecture of the F7 gene in a Spanish population: implication for mapping complex diseases and for functional assaysM Sabater-Lleal, L Almasy, E Martínez-Marchán, et al.
Sangre|August 1, 1994
[Comparative multicenter study of a rabbit high-sensitivity thromboplastin and a recombinant thromboplastin with synthetic phospholipids]F Martínez-Brotóns, M Borrell, J Fontcuberta, et al.
Zeitschrift Fur Gastroenterologie|August 1, 1992
Splenic hematoma in acute pancreatitis. Role of coagulation disordersP Clavé, S Guillaumes, I Blanco, et al.
Thrombosis Research|July 11, 2017
Low ADAMTS13 levels are associated with venous thrombosis risk in womenD Llobet, I Tirado, N Vilalta, et al.
Blood|April 26, 2000
Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosisJ M Soria, L Almasy, J C Souto, et al.
Haematologica|November 6, 2001
Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficienciesI Tirado, J Mateo, J M Soria, et al.
Pageof 18

Showing results (141-150 of 172) with videos related to

Sort By:
Pageof 18
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 24, 2009
SNP sets selection under mutual information criterion, application to F7/FVII datasetH Brunel, A Perera, A Buil, et al.
Stroke|August 30, 2003
Risk of ischemic stroke associated with functional thrombin-activatable fibrinolysis inhibitor plasma levelsA Santamaría, A Oliver, M Borrell, et al.
The Journal of Thoracic and Cardiovascular Surgery|October 1, 1995
Aprotinin versus desmopressin for patients undergoing operations with cardiopulmonary bypass. A double-blind placebo-controlled studyJ I Casas, I Zuazu-Jausoro, J Mateo, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|May 6, 2005
[Renal venous thrombosis in a neonate carrying the G20210A mutation of the prothrombin gene]G M Fraga Rodríguez, R Parody Porras, G Ginovart Galiana, et al.
Clinical Genetics|May 3, 2006
Genetic architecture of the F7 gene in a Spanish population: implication for mapping complex diseases and for functional assaysM Sabater-Lleal, L Almasy, E Martínez-Marchán, et al.
Sangre|August 1, 1994
[Comparative multicenter study of a rabbit high-sensitivity thromboplastin and a recombinant thromboplastin with synthetic phospholipids]F Martínez-Brotóns, M Borrell, J Fontcuberta, et al.
Zeitschrift Fur Gastroenterologie|August 1, 1992
Splenic hematoma in acute pancreatitis. Role of coagulation disordersP Clavé, S Guillaumes, I Blanco, et al.
Thrombosis Research|July 11, 2017
Low ADAMTS13 levels are associated with venous thrombosis risk in womenD Llobet, I Tirado, N Vilalta, et al.
Blood|April 26, 2000
Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosisJ M Soria, L Almasy, J C Souto, et al.
Haematologica|November 6, 2001
Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficienciesI Tirado, J Mateo, J M Soria, et al.
Pageof 18